anti- japanese-encephalitis-viral effects of kaempferol and daidzin and their rna-binding characteristics反japanese-encephalitis-viral山柰酚和黄豆苷及其rna结合特征的影响.pdfVIP
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anti- japanese-encephalitis-viral effects of kaempferol and daidzin and their rna-binding characteristics反japanese-encephalitis-viral山柰酚和黄豆苷及其rna结合特征的影响
Anti- Japanese-Encephalitis-Viral Effects of Kaempferol
and Daidzin and Their RNA-Binding Characteristics
Ting Zhang., Zhiqiang Wu., Jiang Du., Yongfeng Hu, Liguo Liu, Fan Yang*, Qi Jin*
Institute of Pathogen Biology, Chinese Academy of Medical Science Peking Union Medical College, Beijing, China
Abstract
Background: New therapeutic tools and molecular targets are needed for treatment of Japanese encephalitis virus (JEV)
infections. JEV requires an a-1 translational frameshift to synthesize the NS1’ protein required for viral neuroinvasiveness.
Several flavonoids have been shown to possess antiviral activity in vitro against a wide spectrum of viruses. To date, the
antiviral activities of flavonol kaempferol (Kae) and isoflavonoid daidzin (Dai) against JEV have not been described.
Methodology/Principal Findings: The 50% cytotoxic concentration (CC50) and 50% effective concentration (EC50) against
JEV were investigated in BHK21 cells by MTS reduction. Activity against viral genomic RNA and proteins was measured by
real-time RT-PCR and western blotting. The frameshift site RNA-binding characterization was also determined by
electrospray ionization mass spectrometry, isothermal titration calorimetry and autodocking analysis. EC50 values of Kae and
Dai were 12.6 and 25.9 mM against JEV in cells pretreated before infection, whereas in cells infected before treatment, EC50
was 21.5 and 40.4 mM, respectively. Kae exhibited more potent activity against JEV and RNA binding in cells following
internalization through direct inhibition of viral replication and protein expression, indicating that its antiviral activity was
principally due to direct virucidal effects. The JEV frameshift site RNA (fsRNA) was selected as a target for assaying Kae and
Dai. ITC of fsRNA revealed an apparent Kb value for Kae that was nine fold stronger t
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